Canonical Allele Identifier: PA645471850
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 231618
ClinVar RCV Id: RCV000219363 RCV002515630
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Thr234Arg
CA10577945
NM_000251.3:c.701C>G